4.4 Article

Analysis of entire hepatitis B virus genomes reveals reversion of mutations to wild type in natural infection, a 15 year follow-up study

期刊

INFECTION GENETICS AND EVOLUTION
卷 97, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.meegid.2021.105184

关键词

Hepatitis B virus; Evolution; Mutation; Reversion; Next-generation sequencing

资金

  1. Global Health Research Seed Grant from the Carver College of Medicine at the University of Iowa
  2. National Natural Science Foundation of China [81860595, 81703283]
  3. Guangxi Key Research and Development Project [2018AB59002]
  4. Guangxi Natural Science Foundation [2017GXNSFBA198086]

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This study investigated the evolutionary data of HBV genomes using next generation sequencing and found that mutations in HBV may revert to wild type in natural infection. Sequencing of HBV genomes revealed specific mutations in some subjects in 2007, which were absent in 2019.
It has been reported that some mutations in the genome of hepatitis B virus (HBV) may predict the outcome of the virus infection. However, evolutionary data derived from long-term longitudinal analysis of entire HBV genomes using next generation sequencing (NGS) remain rare. In this study, serum samples were collected from asymptomatic hepatitis B surface antigen (HBsAg) carriers from a long-term prospective cohort. The entire HBV genome was amplified by polymerase chain reaction (PCR) and sequenced using NGS. Twenty-eight time series serum samples from nine subjects were successfully analysed. The Shannon entropy (Sn) ranged from 0 to 0.89, with a median value of 0.76, and the genetic diversity (D) ranged from 0 to 0.013, with a median value of 0.004. Intrahost HBV viral evolutionary rates ranged from 2.39E-04 to 3.11E-03. Double mutations at nt1762(A-* T) and 1764(G-* A) and a stop mutation at nt1896(G-* A) were seen in all sequences from subject BO129 in 2007. However, in 2019, most sequences were wild type at these positions. Deletions between nt 2920-3040 were seen in all sequences from subject TS115 in 2007 and 2013 but these were not present in 2004 or 2019. Some sequences from subject CC246 had predicted escape substitutions (T123N, G145R) in the surface protein in 2004, 2013 and 2019 but none of the sequences from 2007 had these changes. In conclusion, HBV mutations may revert to wild type in natural infection. Clinicians should be wary of predicting long-term prognoses on the basis of the presence of mutations.

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